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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596636Generated: October 31, 2026

4-(5-Methoxy-2,2-dimethyl-7-pentyl-2H-1-benzopyran-4-yl)pyridine → HCID 54438745, compound

https://huagongshe.com/reaction/596636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(5-Methoxy-2,2-dimethyl-7-pentyl-2H-1-benzopyran-4-yl)pyridineHCID 21450374—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 54438745HCID 54438745—

Reaction Steps

2,2-Dimethyl-5-methoxy-7-n-pentyl-4-(4-pyridyl)-2H-chromene (3.90g.) was hydrogenated for 4.5 hours at 20° C and 30 p.s.i. in ethanol (100 ml) in the presence of 5% palladium on charcoal (0.50g.). The solution was filtered and evaporated to dryness under reduced pressure to yield 2,2-dimethyl-5-methoxy-7-n-pentyl-4-(4-pyridyl) chroman as a yellow oil (3.90g.). (This compound was also prepared in low yield via treatment of 2,2-dimethyl-7-n-pentyl-4-(4-pyridyl) chroman-5-ol with 1) sodium hydride and 2) iodomethane in benzene).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04011329
Source datasetuspto-grants-1977_03
ORD IDord-806d24ed028443eb9638b87e68cf589c
Source noteuspto-grants-1977_03